Curette Tip. M4X0.5. - Helmut Zepf (24.751.113G)
The POINTE DE CURETTE. M4X0.5. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.113G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 24.751.113G curette tip?
The Helmut Zepf curette tip, referenced under code 24.751.113G, is a manual instrumentation component designed for periodontal and surgical care. Manufactured from medical stainless steel, this tip features a specific M4X0.5 thread allowing it to be mounted on interchangeable instrument handles. This device belongs to Class I of medical devices. Its structure is designed to meet the requirements of oral surgery, offering a rigid and durable interface for the practitioner. As a product of Helmut Zepf Medizintechnik GmbH, it benefits from the expertise of a recognized manufacturer in the field of high-tech dental instrumentation.
What are the clinical indications for this instrument?
This instrument is indicated as a manual dental instrument for various interventions in the dental office or operating room. Its primary use concerns the mechanical removal of infected tissue, deep subgingival scaling, and root planing during periodontal therapies. In implant surgery, it can be used to clean the surgical site or remove granulation tissue. The use of this Helmut Zepf curette tip is strictly reserved for qualified healthcare professionals, ensuring application in accordance with current clinical protocols for the treatment of periodontal pathologies and tissue preparation before implant placement.
What are the technical characteristics of this tip?
The Helmut Zepf curette tip is distinguished by its M4X0.5 threaded connection, ensuring precise compatibility with handles from the same range. It is designed in medical stainless steel, a material chosen for its resistance to sterilization cycles and its relative biological neutrality. The device is delivered non-sterile by Helmut Zepf Medizintechnik GmbH, which requires a complete processing protocol before the first use. The design of the instrument does not define a maximum limit for processing cycles, as the service life depends on visible wear, cracks, or potential damage to the cutting edges observed during preoperative inspection.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this curette tip is the patient's known hypersensitivity or intolerance to metals, specifically medical stainless steel. An allergic reaction may be triggered during contact between the instrument and the patient's tissues. If such a hypersensitivity reaction occurs during the procedure, the manufacturer Helmut Zepf stipulates that the intervention must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before any manipulation with this manual instrument.
What are the maintenance and reprocessing precautions?
Before the first use and after each subsequent use, the curette tip must imperatively be cleaned, disinfected, and sterilized. Helmut Zepf specifies that all products are delivered non-sterile. The practitioner must perform thorough cleaning and check for the absence of visible damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is prohibited as it compromises the safety of care. Although no maximum cycle limit is set due to the robustness of the materials, compatibility with other cleaning and sterilization products must be verified beforehand by the professional.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to associated MDR mentions). Compliance with manufacturing standards guarantees the use of medical stainless steel meeting the requirements of the dental sector. As a Class I instrument, it meets regulatory safety and performance obligations for manual instruments. The reprocessing process is the responsibility of the healthcare professional, who must follow the manufacturer's safety instructions to maintain the integrity of the Helmut Zepf device throughout its useful life.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |



